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The Journal of Physiology|April 23, 2005
A critical role of TRPM channel-kinase for human magnesium transportKarl P Schlingmann, Thomas GudermannPediatric Nephrology (Berlin, Germany)|April 20, 2011
Bartter- and Gitelman-like syndromes: salt-losing tubulopathies with loop or DCT defectsHannsjörg W Seyberth, Karl P SchlingmannBone Reports|December 29, 2018
Juvenile onset IIH and CYP24A1 mutationsKarl P Schlingmann, Walburga Cassar, Martin KonradPflugers Archiv : European Journal of Physiology|August 3, 2005
Essential role for TRPM6 in epithelial magnesium transport and body magnesium homeostasisVladimir Chubanov, Thomas Gudermann, Karl P SchlingmannAmerican Journal of Physiology. Renal Physiology|March 6, 2004
Insights into the molecular nature of magnesium homeostasisMartin Konrad, Karl P Schlingmann, Thomas GudermannJournal of Pediatric Endocrinology & Metabolism : JPEM|September 1, 2020
Idiopathic infantile hypercalcemia: mutations in SLC34A1 and CYP24A1 in two siblings and fathersAyla Güven, Martin Konrad, Karl P SchlingmannPediatric Nephrology (Berlin, Germany)|November 25, 2003
Genetics of hereditary disorders of magnesium homeostasisKarl P Schlingmann, Martin Konrad, Hannsjörg W SeyberthCurrent Opinion in Nephrology and Hypertension|July 27, 2022
The genetic spectrum of Gitelman(-like) syndromesKarl P Schlingmann, Jeroen H F de BaaijJournal of Pediatric Endocrinology & Metabolism : JPEM|June 18, 2008
Autosomal dominant hypoparathyroidism with severe hypomagnesemia and hypocalcemia, successfully treated with recombinant PTH and continuous subcutaneous magnesium infusionSrinath Sanda, Karl P Schlingmann, Ron S NewfieldSaudi Journal of Kidney Diseases and Transplantation : an Official Publication of the Saudi Center for Organ Transplantation, Saudi Arabia|September 18, 2012
Resolving basal ganglia calcification in hereditary hypomagnesemia with secondary hypocalcemia due to a novel TRPM6 gene mutationAbdelhadi M Habeb, Hanan Al-Harbi, Karl P SchlingmannPageof 4